Cloning of a Family 11 Xylanase Gene from Bacillus amyloliquefaciens CH51 Isolated from Cheonggukjangopen access
- Authors
- Baek, C. U.; Lee, S. G.; Chung, Y. R.; Cho, I.; Kim, J. H.
- Issue Date
- Dec-2012
- Publisher
- SPRINGER
- Keywords
- Family 11 xylanase; Bacillus amyloliquefaciens; Overexpression; Purification
- Citation
- INDIAN JOURNAL OF MICROBIOLOGY, v.52, no.4, pp 695 - 700
- Pages
- 6
- Indexed
- SCIE
SCOPUS
- Journal Title
- INDIAN JOURNAL OF MICROBIOLOGY
- Volume
- 52
- Number
- 4
- Start Page
- 695
- End Page
- 700
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/21887
- DOI
- 10.1007/s12088-012-0260-4
- ISSN
- 0046-8991
0973-7715
- Abstract
- Bacillus amyloliquefaciens CH51, an isolate from cheonggukjang, Korean fermented soyfood, secretes several enzymes into culture medium. A gene encoding 19 kDa xylanase was cloned by PCR. Sequencing showed that the gene encoded a glycohydrolase family 11 xylanase and named xynA. xynAHis, xynA with additional codons for his-tag, was overexpressed in Escherichia coli BL21(DE3) using pET-26b(+). XynAHis was purified using HisTrap affinity column. K-m and V-max of XynAHis were 0.363 mg/ml and 701.1 mu mol/min/mg, respectively with birchwood xylan as a substrate. The optimum pH and temperature were pH 4 and 25 A degrees C, respectively. When xynA was introduced into Bacillus subtilis WB600, active XynA was secreted into culture medium.
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